110365743-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: non coding transcript exon variant
orthologous variants: 129182439-A-T

110365820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129182365-T-C

110365870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129182314-G-T

110366103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129182103-G-T

110366445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129181758-A-G

110366445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129181758-A-T

110366474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129181729-T-C

http://identifiers.org/hco/4/GRCh38#110391385-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129175713-A-C

110391707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129175402-C-G

110391707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129175402-C-T

110391744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129175366-G-T

110391757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129175352-T-C

110391830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129175295-G-A

110391866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129175259-T-C

110394872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129175033-A-G

110396466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129174852-G-A

110396467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129174851-C-T

110396910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

110397171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129174502-G-A

http://identifiers.org/hco/4/GRCh38#110397238-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129174450-A-C

110397238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129174450-A-T

110397256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129174432-G-A

110397274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129174414-A-G

110414156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

110414156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-G

110414259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129167081-C-G

110414259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129167081-C-T

110414308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129167028-C-T

110414361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129166964-A-G

http://identifiers.org/hco/4/GRCh38#110414432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129166892-A-C

110414485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129166841-G-C

110414758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129166539-A-G

110414758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129166539-A-T

110414899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129166410-C-T

110415134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129165298-T-C

110415164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129165274-G-C

110423018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129164963-G-A

110423756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129164581-T-G

110423796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129164536-T-C

110423940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129164418-T-C

110423940-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129164418-T-G

110423987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129164371-T-C

110424080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129164006-T-C

110424184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129163785-A-G

110424219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129163754-T-C

110424360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129163632-T-A

110424362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129163630-T-C

110424407-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129163585-T-A

110424490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129163506-C-T

http://identifiers.org/hco/4/GRCh38#110424574-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129163410-A-C

110424577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129163407-T-C

110439851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129162188-A-G

110439990-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129162043-T-A

110440080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129161932-T-C

110442554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129161173-C-T

110447250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129159339-C-T

110447251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129159338-G-A

110450205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129149990-G-A

110450270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129150047-C-T

110453230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129153055-C-T

110453266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129153084-G-T

110453951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129154072-A-T

110454076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129154180-A-T

110454120-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129154212-T-A

110454277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129154344-C-G

http://identifiers.org/hco/4/GRCh38#110454522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129155223-A-C

110454522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129155223-A-G

110454745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129155613-T-A

110458814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129145524-T-C

110458836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129145499-G-T

110459070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129145237-T-C

110459179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129145145-G-A

110459461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129144944-T-C

110459687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129144664-G-T

http://identifiers.org/hco/4/GRCh38#110460077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129144338-C-A

110460077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129144338-C-T

http://identifiers.org/hco/4/GRCh38#110460699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129142672-A-C

110461146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129141645-T-C

110461320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129141491-G-T

110461495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129141307-A-G

110462469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129139224-A-G

110464659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129139043-A-G

110464659-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129139043-A-T

110464937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129138805-C-T

110465343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129138347-T-G

110465745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129137395-G-C

110466043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129137098-C-T

110466075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129137075-C-T

110466667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129136391-C-T

110466945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129136176-T-C

110468768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129134069-G-A

110473027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129130121-G-T

110473227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129129929-G-A

110473273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129129858-T-C

110473311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129129822-T-G

110473890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129128911-T-C

110473946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129128881-T-A

110474559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129128310-A-G

110475627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129126917-T-C

110475702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129126853-T-C

110475840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129126714-A-G

http://identifiers.org/hco/4/GRCh38#110475933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129126608-C-A

110475933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129126608-C-T

110476035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129126511-G-A

110476035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129126511-G-T

110476189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129126337-G-A

110476189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129126337-G-T

http://identifiers.org/hco/4/GRCh38#110476206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129126320-C-A

110476206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129126320-C-G

110476206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129126320-C-T

110476296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129126248-A-G

110476589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129125972-C-T

110476614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129125950-C-T

110476751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129125816-G-A

110476823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129125744-C-T

110476888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 129125679-G-A

110476946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129125621-A-G

http://identifiers.org/hco/4/GRCh38#110477084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129125212-C-A

http://identifiers.org/hco/4/GRCh38#110477104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129125193-C-A

110477104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129125193-C-T

110477210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129125088-A-G

http://identifiers.org/hco/4/GRCh38#110477676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129124634-A-C

110477873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129124410-C-G

110477948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129124338-C-T

http://identifiers.org/hco/4/GRCh38#110478038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129124249-A-C

110478139-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129124148-T-G

110478187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129124098-T-C

110478366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129123964-A-G

110478394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129123953-T-C

110478484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129123884-G-A

110478741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129123763-G-A

110478741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129123763-G-T

110478957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129123542-T-C

110479055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129123454-G-A

110479055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129123454-G-C

110481858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129123220-G-T

110482014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129123088-G-A

http://identifiers.org/hco/4/GRCh38#110482067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129123038-C-A

110482067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129123038-C-G

110482097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129123018-C-T

110482155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129122968-T-C

110483294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129122259-C-G

110483434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129122122-A-G

110483555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129122030-A-G

110483580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129122016-G-A

110483708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129121886-T-G

110483785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129121814-T-C

110484332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129120049-C-T

110484360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129120023-G-A

110484360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129120023-G-T

110484457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129119892-C-T

110484615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129119743-G-A

110485020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129119326-T-C

110487674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129115899-T-C

110487836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129115760-A-G

http://identifiers.org/hco/4/GRCh38#110487943-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129115572-A-C

110488162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129115344-T-C

110488413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129115261-G-A

110488413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129115261-G-C

110488446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129115232-T-C

110488458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129115224-T-A

110488458-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129115224-T-G

110488472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129115210-G-T

110488473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129115209-G-T

110488488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129115194-G-A

110488488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129115194-G-C

110488829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129114864-G-A

110488829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129114864-G-T

110489131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129114581-G-A

110490141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129113967-G-A

110490864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129113314-T-C

110490886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129113293-A-G

http://identifiers.org/hco/4/GRCh38#110490894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129113285-C-A

110490894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129113285-C-T

110490911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129113268-C-G

110490926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129113253-G-A

110490948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129113231-G-A

110490948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129113231-G-T

110490988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129113203-G-A

110490988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129113203-G-T

http://identifiers.org/hco/4/GRCh38#110491028-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129113163-A-C

110491102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129113089-C-T

110491117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129113074-G-A

110491117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129113074-G-C

110491153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129113038-A-G

110491234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129112957-A-G

110491234-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129112957-A-T

110491252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129112939-T-C

http://identifiers.org/hco/4/GRCh38#110491274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129112918-C-A

110491274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129112918-C-G

110491274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129112918-C-T

110491337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129112892-G-A

http://identifiers.org/hco/4/GRCh38#110491635-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129112588-A-C

http://identifiers.org/hco/4/GRCh38#110491700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129112490-C-A

110492334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129111874-T-G

http://identifiers.org/hco/4/GRCh38#110492355-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129111851-A-C

110492367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129111839-T-C

http://identifiers.org/hco/4/GRCh38#110492524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129111690-C-A

110492575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129111645-A-G

110493060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129111194-A-G

110493104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129111150-C-T

110493310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129110975-T-C

110493407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129110880-C-T

110493470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129110821-C-G

110493606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129110710-G-T

110493765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129110576-G-C

110499540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129109022-C-T

110499616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129108948-A-G

110499619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129108945-A-G

110499776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129108751-T-C

110499899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129108625-G-A

110499899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129108625-G-C

http://identifiers.org/hco/4/GRCh38#110500207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129108448-C-A

110504964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129108042-G-A

110504983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129108025-A-G

110505025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129107984-T-C

110505145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129107876-A-G

110505766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129107358-G-T

http://identifiers.org/hco/4/GRCh38#110505827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129107301-C-A

110506043-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129107069-T-A

110506064-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129107048-T-A

http://identifiers.org/hco/4/GRCh38#110506171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129106974-C-A

110506196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129106927-G-T

110506313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129106637-A-G

110506341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129106595-T-G

110506413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129106529-G-T

110506521-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129106444-T-G

110506567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129106401-G-A

110506567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129106401-G-T

http://identifiers.org/hco/4/GRCh38#110506573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129106395-C-A

110506573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129106395-C-G

110506589-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129106373-T-A

110506626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129106338-T-C

110506685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129106280-G-A

110506691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129106274-A-G

110506695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129106270-C-T

110506721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129106244-G-C

110506729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 129106236-T-C

110506752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129106213-A-G

110506754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 129106211-T-C

http://identifiers.org/hco/4/GRCh38#110506841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129106090-C-A

110506932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129106032-T-C

110507203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129105764-T-C

110507227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129105745-C-T

http://identifiers.org/hco/4/GRCh38#110507326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129105640-C-A

110507506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129105484-C-T

110507619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129105413-A-G

110507647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129105376-G-A

110508054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129104915-A-G

110508148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129104819-T-C

http://identifiers.org/hco/4/GRCh38#110508159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129104808-C-A

110508159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129104808-C-T

110508171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129104796-T-C

110508205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129104762-G-A

http://identifiers.org/hco/4/GRCh38#110508297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129104690-C-A

110508297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129104690-C-T

http://identifiers.org/hco/4/GRCh38#110508411-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129104586-A-C

110508478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129104519-A-G

http://identifiers.org/hco/4/GRCh38#110508479-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129104518-A-C

110508479-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129104518-A-T

110509163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129104141-G-A

110509184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129104093-T-C

110509233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129104060-C-G

http://identifiers.org/hco/4/GRCh38#110509348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129103919-C-A

110509348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129103919-C-T

http://identifiers.org/hco/4/GRCh38#110509515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129103706-C-A

110509515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129103706-C-T

110509682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129103541-G-A

110509682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129103541-G-T

110509790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129103433-C-T

110509876-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129103343-T-G

110509889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129103330-A-G

http://identifiers.org/hco/4/GRCh38#110510130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129102879-C-A

110510130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129102879-C-T

110510187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129102837-A-G

110510197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129102826-A-G

http://identifiers.org/hco/4/GRCh38#110510199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129102824-C-A

110510199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129102824-C-T

110510204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129102819-C-G

http://identifiers.org/hco/4/GRCh38#110510434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129102608-A-C

110510434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129102608-A-G

110510510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129102545-T-C

110510510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129102545-T-G

110510636-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129102444-T-A

110510636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129102444-T-C

http://identifiers.org/hco/4/GRCh38#110510640-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129102440-A-C

110510641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129102439-A-G

110510929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129102177-G-A

110510929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129102177-G-T

110511216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129101072-G-A

110511567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129100758-T-C

110511571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129100754-G-A

110511622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129100700-T-C

http://identifiers.org/hco/4/GRCh38#110512062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129100360-C-A

http://identifiers.org/hco/4/GRCh38#110512253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129100183-C-A

110512253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129100183-C-T

http://identifiers.org/hco/4/GRCh38#110512260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129100176-C-A

110512524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129099975-G-T

110512618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129099854-G-C

110512673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129099799-G-T

110512794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129099685-A-G

110512864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129099616-T-C

110512888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129099593-A-G

http://identifiers.org/hco/4/GRCh38#110512901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129099580-C-A

http://identifiers.org/hco/4/GRCh38#110513114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129099417-C-A

110513153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129099390-T-C

http://identifiers.org/hco/4/GRCh38#110513162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129099381-C-A

110513162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129099381-C-T

110513322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129099273-A-T

110513329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129099266-T-C

110513329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129099266-T-G

110513330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129099265-C-T

110513367-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129099228-T-G

110513402-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129099196-T-A

http://identifiers.org/hco/4/GRCh38#110513517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129099086-A-C

110513517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129099086-A-T

110513632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129099001-G-T

110513885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129098911-T-C

http://identifiers.org/hco/4/GRCh38#110513893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129098903-C-A

110513981-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129098809-T-G

110514205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129098535-G-C

110514601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129098235-T-C

110514719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129098131-T-G

110514721-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129098129-A-T

110514985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129097882-T-C

110515132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129097733-C-T

110515268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129097521-A-G

110515279-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129097515-A-T

110515461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129097344-A-G

110515463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129097342-T-C

110515590-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129097197-T-A

110515590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129097197-T-C

110515611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129097176-T-A

110515643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129097144-G-A

110515648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129097139-A-G

110515663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129097124-C-G

110515663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129097124-C-T

110515721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129096963-A-G

110515721-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129096963-A-T

http://identifiers.org/hco/4/GRCh38#110515806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129096885-A-C

http://identifiers.org/hco/4/GRCh38#110515835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129096858-C-A

http://identifiers.org/hco/4/GRCh38#110515870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129096832-C-A

110515870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 129096832-C-G

110515904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129096812-G-A

http://identifiers.org/hco/4/GRCh38#110515946-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129096770-A-C

110515946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129096770-A-G

110515946-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129096770-A-T

http://identifiers.org/hco/4/GRCh38#110515948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129096768-C-A

110515948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129096768-C-T

110515951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129096765-A-T

110515972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129096745-T-A

110515972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129096745-T-C

110515972-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129096745-T-G

110516242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129096515-T-C

110516494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129096223-T-C

110516717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129096003-A-G

http://identifiers.org/hco/4/GRCh38#110517430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129095465-C-A

110517893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129095011-T-C

110518114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129094822-C-T

110518128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129094810-A-G

110518144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129094794-A-G

110518208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129094754-G-A

http://identifiers.org/hco/4/GRCh38#110518654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129094231-C-A

110518723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129094154-G-A

110519115-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129093676-A-T

110519143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129093648-G-T

http://identifiers.org/hco/4/GRCh38#110519151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129093640-C-A

110519151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129093640-C-G

110519216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129093575-A-G

110519236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129093555-T-A

110519239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129093552-G-A

110519271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129093519-G-T

http://identifiers.org/hco/4/GRCh38#110519395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129093411-C-A

110519402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129093404-A-G

110519956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129092854-A-G

http://identifiers.org/hco/4/GRCh38#110519983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129092828-C-A

110519983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129092828-C-T

http://identifiers.org/hco/4/GRCh38#110520104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129092734-C-A

110520121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129092713-A-G

110520278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129092565-C-T

110520579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129092290-A-G

110520711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129092142-T-C

110520746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129092115-C-T

110520971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129091914-C-T

http://identifiers.org/hco/4/GRCh38#110521193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129091717-C-A

http://identifiers.org/hco/4/GRCh38#110521203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129091707-C-A

110521239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129091662-T-G

110523915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129090835-A-G

110523915-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129090835-A-T

110524041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129090738-C-G

110524061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129090718-T-C

110524162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129090623-A-G

110524267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129090555-G-C

110527814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129089590-C-T

110528123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129089309-T-C

110528124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129089308-A-G

110528254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129089182-G-A

110528328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129089106-G-A

110528378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129089048-C-T

110528400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129089020-T-C

110528778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129088640-G-A

110528778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129088640-G-C

110528976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129088454-A-G

110529180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129088265-C-T

110529465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129088054-G-A

110529635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129087909-T-C

110529647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129087890-C-T

110529661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129087878-T-C

110530679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129087353-G-A

110530679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129087353-G-T

110530726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129087311-T-A

110530871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129087232-A-G

110530871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129087232-A-T

110530877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129087226-T-C

110530877-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129087226-T-G

110530939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129087166-G-A

110531057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129087049-A-G

110531057-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129087049-A-T

110531076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129087030-T-C

110531077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129087029-A-G

110531226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129086904-A-G

110531250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129086880-G-A

110531250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129086880-G-T

110531251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129086879-T-A

110531251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129086879-T-C

110531253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129086877-T-C

110531312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129086816-A-G

110531352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129086776-A-G

http://identifiers.org/hco/4/GRCh38#110531354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129086774-C-A

110531354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129086774-C-T

http://identifiers.org/hco/4/GRCh38#110531395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129086732-C-A

110531395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129086732-C-T

110531413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129086714-G-A

110531413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129086714-G-T

110531422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129086705-T-A

110531422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129086705-T-C

110531551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129086582-T-C

110531859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129085996-A-G

110531927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129085932-T-C

110531932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129085927-G-A

110531934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129085925-G-A

110532476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129085281-A-G

110532536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129085207-G-A

110532538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129085205-C-G

110532538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129085205-C-T

110532831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129084851-T-C

110532939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129084777-G-A

http://identifiers.org/hco/4/GRCh38#110532985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129084737-C-A

110533013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129084709-A-G

110533041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129084695-T-C

http://identifiers.org/hco/4/GRCh38#110533114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129084613-C-A

110533165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129084562-C-T

http://identifiers.org/hco/4/GRCh38#110533166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129084561-C-A

110533166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129084561-C-T

110533194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129084530-G-A

110533194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129084530-G-T

110533204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129084520-T-C

http://identifiers.org/hco/4/GRCh38#110533266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129084458-C-A

110533297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129084427-G-A

110533297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129084427-G-T

http://identifiers.org/hco/4/GRCh38#110533359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129084366-C-A

110533454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129084118-T-A

110533454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129084118-T-C

110533454-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129084118-T-G

http://identifiers.org/hco/4/GRCh38#110533469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129084103-A-C

110533469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129084103-A-G

110533480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129084092-T-C

110533481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129084081-G-A

110533481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129084081-G-T

110533570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129083931-G-A

110533570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129083931-G-T

110533578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129083923-A-G

110533743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129083747-C-T

110533833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129083658-A-G

110533833-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129083658-A-T

110534268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129083219-C-T

110534366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129083137-C-T

110534799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129082887-G-A

110534799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129082887-G-T

110534810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129082880-C-T

110534932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129082760-A-G

110535033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129082657-G-T

110535142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129082549-A-G

110540051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129081672-C-G

110540051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129081672-C-T

110540075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129081648-A-T

110540136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129081620-C-T

110540452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129081186-A-T

110540515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129081125-C-T

110540939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129080704-C-G

110541077-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129080574-T-G

110541078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129080573-G-A

110541232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129080419-T-C

110541414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129080255-C-T

110541536-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129080148-T-A

http://identifiers.org/hco/4/GRCh38#110541759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129079911-A-C

110541759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129079911-A-G

110541801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129079869-A-G

110541884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129079794-A-G

110542133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129078659-T-C

110542136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129078656-G-A

110542359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129078222-G-A

110542609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129077977-T-C

110542609-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129077977-T-G

110542694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129077887-T-C

110542695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129077886-C-T

http://identifiers.org/hco/4/GRCh38#110542705-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129077876-A-C

110542705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129077876-A-G

110542763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129077818-A-G

110542763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129077818-A-T

110542843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129077741-G-A

110542846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129077738-A-G

110542861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129077723-G-C

110542895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 129077689-A-G

110542898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129077686-G-A

110542906-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129077676-T-A

110542906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129077676-T-G

110542989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129077592-T-C

110543071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 129077514-G-T

110543177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129077415-A-T

http://identifiers.org/hco/4/GRCh38#110543180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129077412-C-A

110543180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129077412-C-T

110543245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129077334-A-G

110543341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129077233-C-T

110543867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129076555-T-C

110544084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129076346-T-C

110544305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129076115-G-A

http://identifiers.org/hco/4/GRCh38#110548061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129075432-C-A

110548061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129075432-C-T

110548161-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129075356-T-A

110548161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129075356-T-C

110548161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129075356-T-G

110548272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129075245-A-G

110548368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129075148-G-T

http://identifiers.org/hco/4/GRCh38#110548369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129075147-C-A

110548369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129075147-C-G

110548369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129075147-C-T

110548404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129075119-G-A

110548404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129075119-G-T

http://identifiers.org/hco/4/GRCh38#110548405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129075118-C-A

110548405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129075118-C-T

110548432-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129075099-T-A

110548432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129075099-T-C

110548467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129075064-A-G

110548553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129074987-G-C

110548553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129074987-G-T

110548718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129074853-T-C

110549302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129074666-A-G

110549349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129074619-T-C

110549442-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129074525-T-A

110549442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129074525-T-C

110549442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129074525-T-G

110549459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129074508-T-C

110549475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129074489-G-A

110549481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129074483-T-C

110549489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129074475-T-G

110549497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129074467-G-A

110549497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129074467-G-T

110549589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129074375-A-G

110549637-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129074327-T-G

110549680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129074284-T-C

110549720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129074236-C-G

110549720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129074236-C-T

110549843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129074113-C-T

110549892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129074064-T-C

110552507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129071665-C-T

110552531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129071641-A-G

110552663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129071517-A-G

110552747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129071443-C-G

http://identifiers.org/hco/4/GRCh38#110552766-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129071426-A-C

110552766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129071426-A-G

110552932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129071300-G-A

110553228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129070510-G-T

110553394-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129070350-A-T

110553469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129070275-A-G

110553469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129070275-A-T

110553471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129070273-G-C

110553471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129070273-G-T

110553472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129070272-A-G

110553474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129070270-G-A

110553474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129070270-G-T

110553509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129070235-G-A

110553509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129070235-G-C

110553509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129070235-G-T

110553583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129070160-G-A

110553583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129070160-G-T

http://identifiers.org/hco/4/GRCh38#110553586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129070157-C-A

http://identifiers.org/hco/4/GRCh38#110553598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129070034-C-A

110553621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129070007-T-C

http://identifiers.org/hco/4/GRCh38#110553660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129069963-C-A

110553660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129069963-C-T

110553828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129069593-C-G

110554808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 129069144-A-G

http://identifiers.org/hco/4/GRCh38#110555134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129068948-C-A

110555169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129068912-A-G

http://identifiers.org/hco/4/GRCh38#110555292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129068785-A-C

110556010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129068100-C-G

110559525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129065479-G-C

110559525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129065479-G-T

http://identifiers.org/hco/4/GRCh38#110559622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129065093-C-A

http://identifiers.org/hco/4/GRCh38#110559635-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129065082-A-C

110559748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129064969-A-G

110559748-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129064969-A-T

110559762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129064955-G-A

110559762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129064955-G-C

110560490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129064898-C-T

110560567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129064816-G-A

110560651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129064760-C-T

110560653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129064758-C-G

110560653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129064758-C-T

110560807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129064618-T-C

110560863-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129064561-T-A

110560989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129064434-T-C

110561083-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129064346-A-T

http://identifiers.org/hco/4/GRCh38#110561239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129064218-C-A

110561247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129064210-T-C

110561247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129064210-T-G

110561259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129064198-G-T

110561339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129064134-G-C

110561360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129064116-A-G

110561360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129064116-A-T

110561361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129064115-T-G

110561439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129064036-G-A

http://identifiers.org/hco/4/GRCh38#110561550-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129063925-A-C

110561550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129063925-A-G

110561550-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129063925-A-T

110561593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129063875-T-C

110561605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129063863-T-C

110561634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129063834-G-A

110561634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129063834-G-T

http://identifiers.org/hco/4/GRCh38#110561649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129063820-C-A

110561649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129063820-C-T

110561651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129063818-T-A

http://identifiers.org/hco/4/GRCh38#110561664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129063805-A-C

110561664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129063805-A-G

110561693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129063778-T-C

110561792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129063679-A-G

110561792-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129063679-A-T

110561811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129063660-G-T

110562181-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129063293-T-A

http://identifiers.org/hco/4/GRCh38#110562346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129063128-C-A

http://identifiers.org/hco/4/GRCh38#110562388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129063084-C-A

110562388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129063084-C-T

http://identifiers.org/hco/4/GRCh38#110562572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129062924-C-A

110562572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129062924-C-T

http://identifiers.org/hco/4/GRCh38#110562881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129062388-A-C